Long Non-Coding RNA FOXD2-AS1 Serves as a Potential Prognostic Biomarker for Patients With Cancer: A Meta-Analysis and Database Testing

被引:1
|
作者
Duan, Fujiao [1 ]
Li, Hongle [1 ]
Liu, Weigang [3 ]
Zhao, Juanjuan [4 ]
Yang, Zhongyu [5 ]
Zhang, Jianying [2 ]
机构
[1] Zhengzhou Univ, Dept Mol Pathol & Med Res Off, Affiliated Canc Hosp, Zhengzhou, Henan, Peoples R China
[2] Zhengzhou Univ, State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou, Henan, Peoples R China
[3] Hebei Univ Engn, Med Record Stat Off, Affiliated Hosp, Handan, Hebei, Peoples R China
[4] Zhengzhou Univ, Acad Med Sci, Zhengzhou, Henan, Peoples R China
[5] Ohio State Univ, Coll Art & Sci, Columbus, OH USA
来源
关键词
Long non-coding RNA; FOXD2-AS1; Expression; Prognosis; Cancer; Meta-analysis; Am; CELL-PROLIFERATION; INVASION; GLIOMA; BIAS;
D O I
10.1016/j.amjms.2021.01.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The aim of this study is to summarize the current findings concerning the FOXD2-AS1 expression and cancer prognosis. Methods: The correlation intensity between FOXD2-AS1 expression and cancer prognosis was estimated using pooled hazard ratio (HRs) with 95% confidence intervals (CIs). GEPIA was used to assess disease-free survival (DFS), progression-free survival (PFS) and overall survival (OS) of cancer patients and differential FOXD2-AS1 expression in cancer and adjacent tissues. Results: A total of 11 studies including 2,177 patients with OS and 477 patients with DFS/PFS data were analyzed in evidence synthesis. Overall, the pooled analysis indicated that FOXD2-AS1 expression was significantly associated with OS (HR=1.51, 95%Cl: 1.26-1.81, P<0.001) and DFS (HR=1.66, 95%CI: 1.34-2.04, P<0.001). Subgroup analysis showed that high expression of FOXD2-AS1 was significant correlated with poor OS in the median (HR=1.51, 95%CI: 1.30-1.75, P<0.001) and normal group (HR=1.50, 95%CI: 1.09-2.05, 0.01) based on cut-off value, and high FOXD2AS1 expression was significant linked with poor DFS in patients with digestive tract cancer (DTC) (HR=1.66, 95%CI: 1.34-2.04, P<0.001). Similarly, a significant correlation between increased FOXD2-AS1 expression and poor PFS with other cancers (HR=3.84, 95%CI 1.26-11.70, P=0.02) was found. In database testing, a highly significant correlation was observed between high expression of FOXD2-AS1 and poor OS (HR=1.9, P<0.001), but not DFS (HR=1.0, P=0.900). Conclusions: Our findings indicated that FOXD2-AS1 may serve as a potential independent prognostic factor in cancer, especially in the Chinese population.
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收藏
页码:173 / 181
页数:9
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